AccessGUDID - DEVICE: First Aid Only (00092265905657)

GUDID

Device Identifier (DI) Information

Brand Name: First Aid Only
Version or Model: 90565
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 90565
Company Name: Acme United Corporation

Primary DI Number: 00092265905657
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 001180207 *Terms of Use

Device Description: First Aid Kit, 50 Person bulk with Plastic case. Contains: Adhesive Plastic Bandages 1" x 3" (60), Alcohol Pads (20), Burn Dressing 4" x 4", Antiseptic Towelettes (15), Cold Pack4" x 5", Conforming Gauze Roll “2" (2), Conforming Gauze Roll 4", CPR Face Shield, Elastic Bandage 2" x 5yd, Eyewash 1oz bottle, Fingertip Fabric Bandages (10), First Aid Guide, First Aid Tape 1/2" x 5yd, First Aid/Burn Cream Packets (12), Hand Sanitizer Packets (10), Knuckle Fabric Bandages (10), Nitrile Exam Gloves (4), Povidone-Iodine Wipes (4), Scissors, Sterile Eye Pads (2), Sterile Gauze Pads 3" x 3" (6), Sting Relief Wipes (3), Trauma Pads 5" x 9" (2), Triangular Bandage 40" x 40" x 56", Triple Antibiotic Ointment Packets (12), Tweezers

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
Kit:	Yes
Combination Product:	Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
44039	First aid kit, medicated	A convenient collection of equipment, materials and pharmaceuticals intended to be used in an emergency for the rapid, initial treatment of an injury. It is typically used by emergency medical services (EMS), hospitals, institutions, schools, and other public settings. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LRR	First Aid Kit With Drug

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 183005f4-7501-4d98-926f-71ea7999a8a7
Public Version Date: April 15, 2021
Public Version Number: 2
DI Record Publish Date: September 16, 2020